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Phylogenetic Relationships and the Larval Head of the Lower Cyclorrhapha (Diptera)
Zoological Journal of the Linnean Society, 2008, 153, 287–323. With 25 figures Phylogenetic relationships and the larval head of the lower Cyclorrhapha (Diptera) GRAHAM E. ROTHERAY1* and FRANCIS GILBERT2 1National Museums of Scotland, Chambers Street, Edinburgh EH1 1JF, UK 2School of Biology, University of Nottingham, Nottingham NR7 2RD, UK Received 23 April 2007; accepted for publication 1 August 2007 We examined final-stage larvae of all currently recognized lower cyclorrhaphan (= Aschiza) families, except Ironomyiidae and Sciadoceridae, and those of the higher cyclorrhaphan (= Schizophora) families Calliphoridae, Conopidae, Lonchaeidae, Muscidae, and Ulidiidae, and compared them with larvae of two out-group families, Rhagionidae and Dolichopodidae, paying particular attention to structures of the head. A set of 86 morphological characters were analysed phylogenetically. The results show that the lower Cyclorrhapha is paraphyletic in relation to the higher Cyclorrhapha. The monophyly of the Cyclorrhapha is strongly supported. The lower Cyclorrhapha is resolved into two clades, based on the Lonchopteridae. Within the Syrphidae the traditional three-subfamily system is supported, based on the Microdontinae. Within the lower Cyclorrhapha, the larval head is variable in form and arrangement of components. In Lonchopteridae, the mouth lies at the back of an open trough or furrow, comprising ventrally an elongate labium and laterally the maxilla. This arrangement of components appears to facilitate scooping food in water films. In Platypezoidea there is no furrow, and the dorsolateral lobes bearing the antennae are connected by a dorsal extension of the pseudocephalon. The main food-gathering structure is the hooked apex of the labium, but in Phoridae the mandibles may also be important. -
Hymenoptera: Formicidae) of Zakynthos Island, Greece
ANNALS OF THE UPPER SILESIAN MUSEUM IN BYTOM ENTOMOLOGY Vol. 27 (online 004): 1–13 ISSN 0867-1966, eISSN 2544-039X (online) Bytom, 9.11.2018 LECH BOROWIEC1 , SEBASTIAN SALATA1,2 Notes on ants (Hymenoptera: Formicidae) of Zakynthos Island, Greece http://doi.org/10.5281/zenodo.1481794 1 Department of Biodiversity and Evolutionary Taxonomy, University of Wrocław, Przybyszewskiego 65, 51-148 Wrocław, Poland e-mail: 1 [email protected], 2 [email protected] Abstract: Forty five ant species were recorded from the Zakynthos Island (Ionian Islands) in 2018, including seven not attributed to any formally described taxon. A comparison of ant fauna of Zakynthos with ant fauna of Samos islands is presented. Both islands have similar surface area (405.6 versus 476.4 km2) and are placed almost on the same latitude (37°) but represent the most western and the most eastern fauna complexes in Greece; 78 species and morphospecies were recorded from both islands but only 23 species are common. Key words: ants, Greece, East Aegean Islands, Samos, faunistics, taxonomy. INTRODUCTION Zakynthos is a Greek island placed in the Ionian Sea. It is the third largest of the Ionian Islands, placed 13.5 km south of Kephalonia – the largest Ionian island, and 18 km west of the Peloponnese. It is also a separate regional unit of the Ionian Islands Region. The area of the island is 405.55 km2 and it is 37 km long and 19 km wide. Its coastline is roughly 123 km. The island is very diverse, with a mountainous plateau on its western half, steep cliffs on southwest coast, and densely populated and fertile plain, with long sandy beaches and several isolated hills, on the eastern part. -
Lasius Fuliginosus (Hymenoptera: Formicidae) Shapes Local Ant Assemblages
NORTH-WESTERN JOURNAL OF ZOOLOGY 10 (2): 404-412 ©NwjZ, Oradea, Romania, 2014 Article No.: 141104 http://biozoojournals.ro/nwjz/index.html Lasius fuliginosus (Hymenoptera: Formicidae) shapes local ant assemblages Piotr ŚLIPIŃSKI1,*, Bálint MARKÓ2, Kamil RZESZOWSKI1, Hanna BABIK1 and Wojciech CZECHOWSKI1 1. Museum and Institute of Zoology, Polish Academy of Sciences, Wilcza 64, 00-679 Warsaw, Poland, E-mails: [email protected], [email protected], [email protected], [email protected]. 2. Hungarian Department of Biology and Ecology, Babeş-Bolyai University, Clinicilor str. 5-7, 400006 Cluj-Napoca, Romania, E-mail: [email protected]. * Corresponding author, P. Ślipiński, E-mail: [email protected] Received: 20. December 2013 / Accepted: 22. March 2014 / Available online: 17. October 2014 / Printed: December 2014 Abstract. Interspecific competition is a major structuring force in ant assemblages. The assemblages are organized hierarchically, with territorial species as top competitors. In boreal areas and in the temperate deciduous forest biome common territorials are species of the subgenus Formica s. str. They are well known for their negative impact on lower-ranked ant species. Less is known, though the structuring role of Lasius fuliginosus, another territorial ant species. Some earlier studies have shown or suggested that it may restrictively affect subordinate species (including direct predation toward them) even stronger than wood ants do. In the present study we compared species compositions and nest densities of subordinate ant species within and outside territories of L. fuliginosus. The results obtained confirmed that this species visibly impoverishes both qualitatively (reduced species richness, altered dominance structures) and quantitatively (decreased nest densities) ant assemblages within its territories. -
Effect of Formica Aserva Forel (Hymenoptera: Formicidae) on Ground Dwelling Arthropods in Central British Columbia
EFFECT OF FORMICA ASERVA FOREL (HYMENOPTERA: FORMICIDAE) ON GROUND DWELLING ARTHROPODS IN CENTRAL BRITISH COLUMBIA by Kendra Gail Schotzko B.S., University of Idaho, 2008 THESIS SUBMITTED IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF MASTER OF SCIENCE IN NATURAL RESOURCES AND ENVIRONMENTAL STUDIES (BIOLOGY) UNIVERSITY OF NORTHERN BRITISH COLUMBIA June 2012 © Kendra G. Schotzko, 2012 Library and Archives Bibliotheque et Canada Archives Canada Published Heritage Direction du 1+1 Branch Patrimoine de I'edition 395 Wellington Street 395, rue Wellington Ottawa ON K1A0N4 Ottawa ON K1A 0N4 Canada Canada Your file Votre reference ISBN: 978-0-494-94131-7 Our file Notre reference ISBN: 978-0-494-94131-7 NOTICE: AVIS: The author has granted a non L'auteur a accorde une licence non exclusive exclusive license allowing Library and permettant a la Bibliotheque et Archives Archives Canada to reproduce, Canada de reproduire, publier, archiver, publish, archive, preserve, conserve, sauvegarder, conserver, transmettre au public communicate to the public by par telecommunication ou par I'lnternet, preter, telecommunication or on the Internet, distribuer et vendre des theses partout dans le loan, distrbute and sell theses monde, a des fins commerciales ou autres, sur worldwide, for commercial or non support microforme, papier, electronique et/ou commercial purposes, in microform, autres formats. paper, electronic and/or any other formats. The author retains copyright L'auteur conserve la propriete du droit d'auteur ownership and moral rights in this et des droits moraux qui protege cette these. Ni thesis. Neither the thesis nor la these ni des extraits substantiels de celle-ci substantial extracts from it may be ne doivent etre imprimes ou autrement printed or otherwise reproduced reproduits sans son autorisation. -
Ants Inhabiting Oak Cynipid Galls in Hungary
North-Western Journal of Zoology 2020, vol.16 (1) - Correspondence: Notes 95 Ants inhabiting oak Cynipid galls in Hungary Oaks are known to harbour extremely rich insect communi- ties, among them more than 100 species of gall wasps (Hy- menoptera: Cynipidae) in Europe (Csóka et al. 2005, Melika 2006). Some gall wasp species are able to induce large and structurally complex galls that can sometimes be abundant on oaks, providing attractive shelters for several arthropod taxa including ant species. Ants are among the most important players in many ecosystems and they are also considered to act as ecosystem engineers (Folgarait, 1998). They are also famous for having ecological or physical interactions with a great variety of other organisms, such as gall wasps. Ants are known to tend Figure 1. Inner structure of the asexual Andricus quercustozae gall in- aphid colonies on the developing galls and, as general pred- habited by ants. ators, they prey on arthropods approaching the protected aphid colonies. Some oak cynipid galls secrete honeydew on their surface. This sweet substrate attracts ants and, in re- turn, the ants protect the galls from predators and parasi- toids (Abe, 1988, 1992; Inouye & Agrawal 2004; Nicholls, 2017). Beyond this obvious ecological interaction between gall wasps and ants, this association continues after the gall wasp’s life cycle has ceased. Certain galls are known to serve as either temporary or permanent shelter for many ant species. Some galls (e.g. An- dricus hungaricus (Hartig), Andricus quercustozae (Bosc), Aphelonyx cerricola (Giraud)) are large enough even for re- productive ant colonies. The advantages of galls as nesting logs are multifaceted. -
Fecundity of Ant Queens in Relation to Their Age and the Mode of Colony Founding L
Insectes Sociaux, Paris Masson, Paris, 1990 1990, Volume 37, n ~ 2, pp. 116-130 FECUNDITY OF ANT QUEENS IN RELATION TO THEIR AGE AND THE MODE OF COLONY FOUNDING L. KELLER (1) and L. PASSERA (2) (1) Musde Zoologique, Palais de Rumine, CP 448, 1000 Lausanne 17, Switzerland (2) Laboratoire d'Entomologie, Universitd Paul Sabatier, 118, route de Narbonne, F 31062 Toulouse Cedex, France, U.A. C.N.R.S. 303 Regu le 23 janvier 1989 Accept6 le 15 juin 1989 SUMMARY The change over time in the fecundity and weight of queens was investigated in three monogynous, independent colony founding species, Lasius niger, Camponotus ligniperda and C. herculaneus, and two polygynous dependent colony founding species, Plagiolepis pygmaea and Iridomyrmex humilis. Queens of the three species founding independently exhibited a similar pattern with a significant loss of weight between mating and the emergence of the first workers. In contrast, weights of queens of the species employing dependent colony founding remained more stable. Fecundity of queens founding inde- pendently increased slowly with time whereas fecundity of queens founding dependently reached the maximum level some weeks after the beginning of the first reproductive season. These results are discussed in relation to some differences in the life history (e.g., life-span) between queens utilizing independent and dependent colony founding. RESUME Fdcondit6 des reines de fourmis en relation avec leur &ge et le mode de fondation de la soci6t6 On a 6tud6 dans ce travail les variations en fonction du temps de la f6condit6 et du poids des reines fondatrices de trois esp6ces monogynes h fondation ind6pendante (Lasius niger, Camponotus ligniperda, Camponotus herculeanus) et de deux esp6ces polygynes h fondation d6pendante (Plagiolepis pygmaea et Iridomyrmex humilis). -
Dipterists Forum
BULLETIN OF THE Dipterists Forum Bulletin No. 76 Autumn 2013 Affiliated to the British Entomological and Natural History Society Bulletin No. 76 Autumn 2013 ISSN 1358-5029 Editorial panel Bulletin Editor Darwyn Sumner Assistant Editor Judy Webb Dipterists Forum Officers Chairman Martin Drake Vice Chairman Stuart Ball Secretary John Kramer Meetings Treasurer Howard Bentley Please use the Booking Form included in this Bulletin or downloaded from our Membership Sec. John Showers website Field Meetings Sec. Roger Morris Field Meetings Indoor Meetings Sec. Duncan Sivell Roger Morris 7 Vine Street, Stamford, Lincolnshire PE9 1QE Publicity Officer Erica McAlister [email protected] Conservation Officer Rob Wolton Workshops & Indoor Meetings Organiser Duncan Sivell Ordinary Members Natural History Museum, Cromwell Road, London, SW7 5BD [email protected] Chris Spilling, Malcolm Smart, Mick Parker Nathan Medd, John Ismay, vacancy Bulletin contributions Unelected Members Please refer to guide notes in this Bulletin for details of how to contribute and send your material to both of the following: Dipterists Digest Editor Peter Chandler Dipterists Bulletin Editor Darwyn Sumner Secretary 122, Link Road, Anstey, Charnwood, Leicestershire LE7 7BX. John Kramer Tel. 0116 212 5075 31 Ash Tree Road, Oadby, Leicester, Leicestershire, LE2 5TE. [email protected] [email protected] Assistant Editor Treasurer Judy Webb Howard Bentley 2 Dorchester Court, Blenheim Road, Kidlington, Oxon. OX5 2JT. 37, Biddenden Close, Bearsted, Maidstone, Kent. ME15 8JP Tel. 01865 377487 Tel. 01622 739452 [email protected] [email protected] Conservation Dipterists Digest contributions Robert Wolton Locks Park Farm, Hatherleigh, Oakhampton, Devon EX20 3LZ Dipterists Digest Editor Tel. -
Observations on the Mobility of the Silver-Studded Blue Plebejus Argus [Online]
30 October 2019 © Harry E. Clarke Citation: Clarke, H.E. (2019). Observations on the Mobility of the Silver-studded Blue Plebejus argus [Online]. Available from http://www.dispar.org/reference.php?id=150 [Accessed November 15, 2019]. Observations on the Mobility of the Silver-studded Blue Plebejus argus Harry E. Clarke Abstract: The Silver-studded Blue is often considered to be a sedentary species, not moving more than 50 m during its life. However, based on recent research and my own experience from Surrey, this is not the case. Males can easily move 200 m when relocated away from ant nests, and new sites can be colonised within a few years from source sites at least 3 km away, probably a year or so after the ants Lasius niger or Lasius alienus have colonised. Silver-studded Blue is a butterfly of early successional habitat, so it needs to be mobile in order to find suitable habitat for the next generation. If it was very sedentary, then colonies would soon die out as habitat matures and becomes unsuitable to support the ants and the butterfly. Introduction This article has been prompted by the statements that Silver-studded Blue (Plebejus argus) is sedentary, barely moving more than 20 m, with 50 m considered exceptional, and breeding populations of 100 m or more considered isolated, based on three mark-release-recapture studies (Thomas, 2014) and (Eeles, 2019). This does not agree with my own observations and does not seem consistent with the habitat requirements. Figure 1 - Male Silver-studded Blue on Bell Heather Photo © Harry E. -
Succession in Ant Communities (Hymenoptera: Formicidae) in Deciduous Forest Clear-Cuts – an Eastern European Case Study
EUROPEAN JOURNAL OF ENTOMOLOGYENTOMOLOGY ISSN (online): 1802-8829 Eur. J. Entomol. 114: 92–100, 2017 http://www.eje.cz doi: 10.14411/eje.2017.013 ORIGINAL ARTICLE Succession in ant communities (Hymenoptera: Formicidae) in deciduous forest clear-cuts – an Eastern European case study IOAN TĂUŞAN 1, JENS DAUBER 2, MARIA R. TRICĂ1 and BÁLINT MARKÓ 3 1 Department of Environmental Sciences, Lucian Blaga University of Sibiu; Applied Ecology Research Centre, Dr. Raţiu 5-7, 550012 Sibiu, Romania; e-mails: [email protected], [email protected] 2 Thünen Institute of Biodiversity, Federal Research Institute for Rural Areas, Forestry and Fisheries, Bundesallee 50, D-38116 Braunschweig, Germany; e-mail: [email protected] 3 Hungarian Department of Biology and Ecology, Babeş-Bolyai University, Clinicilor 5-7, 400006 Cluj-Napoca, Romania; e-mails: [email protected], [email protected] Key words. Hymenoptera, Formicidae, ants, deciduous forests, secondary succession, clear-cutting, community structure, pitfall traps Abstract. Clear-cutting, the main method of harvesting in many forests in the world, causes a series of dramatic environmental changes to the forest habitat and removes habitat resources for arboreal and epigeal species. It results in considerable changes in the composition of both plant and animal communities. Ants have many critical roles in the maintenance and functioning of forest ecosystems. Therefore, the response of ants to clear-cutting and the time it takes for an ant community to recover after clear- cutting are important indicators of the effect of this harvesting technique on the forest ecosystem. We investigated ground-dwelling ant communities during secondary succession of deciduous forests in Transylvania, Romania. -
The Ants of Oklahoma Master of Science
THE ANTS OF OKLAHOMA By Jerry H. Young(I\" Bachelor of Science Oklahoma Agricultural and Mechanical College Stillwater, Oklahoma 1955 Submitted to the faculty of the Graduate School of the Oklahoma Agricultural and Mechanical College in partial fulfillment of the requirements for the degree of MASTER OF SCIENCE January 1 1956 tl<lAWMA AGCMCl«.f�Al L �Ci'!AlttCAl e&U.Ull LIBRARY JUL16195 6 THE ANTS OF OKLAHOMA Thesis Approved: Thesis Adviser }>JcMem��f � 't'" he Thesis ) Committee Member of the Thesis Committee 7'4'.��Member of the Thesis Committee Head of the Department ifean of the Graduate School 361565 ii PREFACE The study of the distribution of ants in the United States has been a long and continuous process with many contributors, but the State of Oklahoma has not received the attentions of these observers to any great extent. The only known list of ants of Oklahoma is one prepared by Mo Ro Smith (1935)0 Early in 1954 a survey of the state of Oklahoma was made to determine the species present and their distributiono The results of this survey, which blanketed the entire State, are given in this paper. The author wishes to express his appreciation to Dro Do E. Howell, chairman of the writer's thesis committee, for his valuable assistance and careful guidance in the preparation of this papero Also, much guidance on preparation of this manuscrip_t was received from Drs. Do Eo Bryan, William H. Irwin and F. A. Fenton. Many of the determin ations were made by M. R. Smith.. Vital infonnation was obtained from the museums at Oklahoma Agricultural and Mechanical College and the University of Oklahoma. -
Final Report 1
Sand pit for Biodiversity at Cep II quarry Researcher: Klára Řehounková Research group: Petr Bogusch, David Boukal, Milan Boukal, Lukáš Čížek, František Grycz, Petr Hesoun, Kamila Lencová, Anna Lepšová, Jan Máca, Pavel Marhoul, Klára Řehounková, Jiří Řehounek, Lenka Schmidtmayerová, Robert Tropek Březen – září 2012 Abstract We compared the effect of restoration status (technical reclamation, spontaneous succession, disturbed succession) on the communities of vascular plants and assemblages of arthropods in CEP II sand pit (T řebo ňsko region, SW part of the Czech Republic) to evaluate their biodiversity and conservation potential. We also studied the experimental restoration of psammophytic grasslands to compare the impact of two near-natural restoration methods (spontaneous and assisted succession) to establishment of target species. The sand pit comprises stages of 2 to 30 years since site abandonment with moisture gradient from wet to dry habitats. In all studied groups, i.e. vascular pants and arthropods, open spontaneously revegetated sites continuously disturbed by intensive recreation activities hosted the largest proportion of target and endangered species which occurred less in the more closed spontaneously revegetated sites and which were nearly absent in technically reclaimed sites. Out results provide clear evidence that the mosaics of spontaneously established forests habitats and open sand habitats are the most valuable stands from the conservation point of view. It has been documented that no expensive technical reclamations are needed to restore post-mining sites which can serve as secondary habitats for many endangered and declining species. The experimental restoration of rare and endangered plant communities seems to be efficient and promising method for a future large-scale restoration projects in abandoned sand pits. -
Elizabeth I. Cash
ELIZABETH I. CASH Department of Environmental Science, Policy, and Management University of California, Berkeley 130 Mulford Hall, #3114 Berkeley, CA 94720-3114 Email: [email protected] URL: http://www.elizabethcash.com/ CURRENT POSITION University of California, Berkeley Berkeley, CA Postdoctoral Scholar August 2016 - Present EDUCATION Arizona State University Tempe, AZ PhD, Biology 2016 Dissertation: Proximate and ultimate mechanisms of nestmate recognition in ants Advisors: Jürgen Gadau (committee chair) & Jürgen Liebig Committee: Jennifer Fewell, Bert Hölldobler, & Kenro Kusumi The Ohio State University Columbus, OH BSc, cum laude, Biology 2009 Independent Research: The function of pheromones in socially parasitic Lasius ants Advisors: Joseph Raczkowski, Steven Rissing, & John Wenzel University of Cincinnati Cincinnati, OH Foundation Coursework, Design 1999 RESEARCH EXPERIENCE AND TRAINING University of California, Berkeley Berkeley, CA Postdoctoral Scholar; Advisor: Neil D. Tsutsui August 2016 - Present Evolution of desiccation resistance and colony recognition in Argentine ants Arizona State University Tempe, AZ Graduate Research Associate; Advisor: Jürgen Gadau 2009 - 2016 Acyl-CoA desaturase gene family evolution and function in ants Ant Course Portal, AZ Participant; Field course on ant collection, identification, and curation 2015 University of Würzburg / Arizona State University Würzburg, Germany Participant; International symposium and workshop on frontiers in insect biology 2014 Smithsonian Tropical Research Institute / Arizona State University BCI, Panama Participant; Tropical Field Biology course 2011 The Ohio State University Columbus, OH Laboratory Assistant; Advisors: Joseph Raczkowski, Steven Rissing, & John Wenzel 2007 - 2009 Behavioral and chemical ecology of social parasitism in Lasius ants 1 PEER-REVIEWED PUBLICATIONS Cash E, Tsutsui N, and Smith A (in preparation) The evolution of acyl-CoA desaturase genes in Odontomachus trap-jaw ants.